Canonical Allele Identifier: CA400353296

Gene: RAD51C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58709878A>T , CM000679.2:g.58709878A>T	GRCh38
NC_000017.10:g.56787239A>T , CM000679.1:g.56787239A>T	GRCh37
NC_000017.9:g.54142238A>T	NCBI36
NG_023199.1:g.22277A>T , LRG_314:g.22277A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_058216.3:c.725A>T MANE Select	NP_478123.1:p.Asp242Val
ENST00000337432.9:c.725A>T MANE Select	ENSP00000336701.4:p.Asp242Val
NM_058216.2:c.725A>T	NP_478123.1:p.Asp242Val
NR_103872.1:n.629A>T
NR_103872.2:n.600A>T
ENST00000337432.8:c.725A>T	ENSP00000336701.4:p.Asp242Val
ENST00000413590.5:c.363A>T
ENST00000461271.5:c.374A>T	ENSP00000464056.1:p.Asp125Val
ENST00000461271.6:c.374A>T	ENSP00000464056.2:p.Asp125Val
ENST00000475762.5:c.*1428A>T	ENSP00000432421.1:n.*1428A>T
ENST00000482007.5:c.*153A>T	ENSP00000433332.1:n.*153A>T
ENST00000487525.5:c.*298A>T	ENSP00000431637.1:n.*298A>T
ENST00000578151.1:n.60A>T
ENST00000581221.5:n.240A>T
ENST00000583539.5:c.725A>T	ENSP00000463121.1:p.Asp242Val
ENST00000584617.5:c.447A>T
ENST00000584804.1:c.20A>T	ENSP00000463658.1:p.Asp7Val
ENST00000697678.1:n.627A>T
ENST00000697679.1:n.1799A>T
ENST00000697680.1:c.*1589A>T	ENSP00000513392.1:n.*1589A>T
ENST00000697681.1:c.*1886A>T	ENSP00000513393.1:n.*1886A>T
ENST00000697683.1:c.*1589A>T	ENSP00000513395.1:n.*1589A>T
ENST00000697684.1:n.785A>T
ENST00000697685.1:c.*1422A>T	ENSP00000513396.1:n.*1422A>T
ENST00000697686.1:c.374A>T	ENSP00000513397.1:p.Asp125Val
ENST00000697687.1:n.604A>T
ENST00000697688.1:n.771A>T
ENST00000697689.1:c.*1261A>T	ENSP00000513398.1:n.*1261A>T
ENST00000697690.1:c.725A>T	ENSP00000513399.1:p.Asp242Val
ENST00000697691.1:c.*697A>T	ENSP00000513400.1:n.*697A>T
ENST00000697692.1:c.*737A>T	ENSP00000513401.1:n.*737A>T
ENST00000697694.1:c.374A>T	ENSP00000513402.1:p.Asp125Val
ENST00000697695.1:n.1332A>T
XM_006722001.2:c.725A>T	XP_006722064.1:p.Asp242Val
XM_006722001.4:c.725A>T	XP_006722064.1:p.Asp242Val
XM_006722002.2:c.725A>T	XP_006722065.1:p.Asp242Val
XM_006722002.4:c.725A>T	XP_006722065.1:p.Asp242Val
XM_006722004.2:c.374A>T	XP_006722067.1:p.Asp125Val
XM_006722004.3:c.374A>T	XP_006722067.1:p.Asp125Val
XM_006722005.2:c.374A>T	XP_006722068.1:p.Asp125Val
XM_006722005.3:c.374A>T	XP_006722068.1:p.Asp125Val
XM_011525092.1:c.374A>T	XP_011523394.1:p.Asp125Val
XM_011525092.2:c.374A>T	XP_011523394.1:p.Asp125Val
XM_011525093.1:c.374A>T	XP_011523395.1:p.Asp125Val
XM_011525093.2:c.374A>T	XP_011523395.1:p.Asp125Val
XM_011525094.1:c.374A>T	XP_011523396.1:p.Asp125Val
XM_011525094.2:c.374A>T	XP_011523396.1:p.Asp125Val
XM_017024914.1:c.374A>T	XP_016880403.1:p.Asp125Val
XM_017024915.1:c.374A>T	XP_016880404.1:p.Asp125Val
XM_017024916.1:c.374A>T	XP_016880405.1:p.Asp125Val
XM_017024917.1:c.374A>T	XP_016880406.1:p.Asp125Val
XM_017024918.2:c.374A>T	XP_016880407.1:p.Asp125Val
XM_017024919.1:c.374A>T	XP_016880408.1:p.Asp125Val
XR_934513.1:n.943A>T
XR_934513.3:n.1374A>T
XR_934514.1:n.943A>T
XR_934514.3:n.1374A>T